首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Prophage lambda induction of Escherichia coli K12 envA uvrB: a highly sensitive test for potential carcinogens.
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Prophage lambda induction of Escherichia coli K12 envA uvrB: a highly sensitive test for potential carcinogens.

机译:大肠杆菌K12 envA uvrB的噬菌体λ诱导:对潜在致癌物的高度敏感测试。

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摘要

A simple, inexpensive, and sensitive test for potential carcinogens based upon the property of carcinogens to induce prophage lambda is described. By using chemicals activated with microsomal enzymes and E. coli K12 permeable (envA) tester bacteria also deficient in DNA repair (uvrB), the range of carcinogens detected in a lysogenic induction test (inductest) has been extended. We have provided the evidence that, after activation, carcinogenic polycyclic hydrocarbons such as benzo[a5pyrene and 7,12-dimethylbenz[a]anthracene induce prophage lambda. Three variants of the test have been developed (inductests I, II, and III), which are as sensitive as the mutagenicity test of Ames et al. [Ames, B. N., McCann, J. and Yamasaki, E. (1975) Mutat. Res. 31, 347-364]. Inductests II and III provide a quantitative estimation of the inducing activity of a carcinogen. With the latter test, one can determine: (i) the cellular toxic effect of a carcinogen and (ii) the kinetics of appearance and disappearance of active metabolites. For two series of chemicals, aflatoxins and benz[a]anthracenes, there is a good correlation between their carcinogenic activity in rodents and their prophage inducing activity in bacteria. The fact that the majority of the cell population is induced makes it possible to test the inducing activity of carcinogens at the biochemical level, e.g., by measuring lambda repressor inactivation.
机译:描述了一种基于致癌物诱导前兆λ的特性的潜在致癌物的简单,廉价且敏感的测试。通过使用由微粒体酶和同样缺乏DNA修复(uvrB)的大肠杆菌K12渗透性(envA)测试细菌激活的化学物质,在溶源诱导测试(诱导剂)中检测到的致癌物范围得到了扩展。我们提供的证据表明,活化后,致癌的多环烃(例如苯并[a5 re]和7,12-二甲基苯并[a]蒽)会诱发前噬菌素。已经开发了该测试的三种变体(诱导剂I,II和III),其敏感性与Ames等人的诱变性测试一样。 [Ames,B. N.,McCann,J.和Yamasaki,E.(1975)Mutat。 Res。 31,347-364]。诱导物II和III提供了对致癌物诱导活性的定量估计。通过后一种测试,可以确定:(i)致癌物的细胞毒性作用和(ii)活性代谢物出现和消失的动力学。对于黄曲霉毒素和苯并[a]蒽这两种化学物质,它们在啮齿动物中的致癌活性与细菌中的腐殖酸诱导活性之间具有良好的相关性。诱导了大多数细胞群的事实使得可以在生化水平上测试致癌物的诱导活性,例如通过测量λ阻遏物的失活。

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